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首页> 外文期刊>Plant Molecular Biology Reporter >Identification and Molecular Characterization of Homeologous Δ9-Stearoyl Acyl Carrier Protein Desaturase 3 Genes from the Allotetraploid Peanut (Arachis hypogaea)
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Identification and Molecular Characterization of Homeologous Δ9-Stearoyl Acyl Carrier Protein Desaturase 3 Genes from the Allotetraploid Peanut (Arachis hypogaea)

机译:异源四倍体花生同源基因Δ9-硬脂酰基酰基载体蛋白去饱和酶3基因的鉴定与分子特征

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The stearoyl–acyl carrier protein (ACP) desaturase (SAD) is a nuclear-encoded, plastid-localized soluble desaturase that catalyzes the conversion of stearoyl-ACP to oleoyl-ACP and plays a key role in the determination of the properties of the majority of cellular glycerolipids. Sad genes from a variety of plant species have been cloned and characterized. However, in peanut (Arachis hypogaea), an important edible and oilseed crop, these genes have not yet been characterized. By searching peanut expressed sequence tag (EST) and parallel sequencing (454) libraries, we have identified three members of the ahSad gene family. Among them, only one gene, ahSad3, was exclusively expressed during seed development and in a manner fully corresponding to oil accumulation. Both ahSad3 homeologous genes (ahSad3A and ahSad3B) were recovered from the allotetraploid peanut, and their mRNA expression levels were characterized. The open reading frames for ahSad3A and ahSad3B are 98% identical and consist of 1,158 bp, encoding a 386-full-amino-acid protein, with one intron in the coding sequence. Comparisons of the sequences of these two homeologous genes revealed seven single-nucleotide polymorphisms and one triplet insertion in the coding region. Southern blot analysis indicated that there are only two copies of the ahSad3 gene in the peanut genome. Homeolog-specific gene expression analysis showed that both ahSad3 homeologs are expressed in developing seeds, but gene expression is significantly biased toward the B genome. Our results point to ahSad3 as a possible target gene for manipulation of fatty acid saturation in A. hypogaea.
机译:硬脂酰基-酰基载体蛋白(ACP)去饱和酶(SAD)是一种核编码的,质体定位的可溶性去饱和酶,可催化硬脂酰基-ACP转化为油酰基-ACP,并在确定大多数蛋白质的性质中起关键作用细胞甘油脂。已经克隆并鉴定了来自多种植物物种的悲伤基因。但是,在重要的食用和油料作物花生(花生)中,这些基因尚未鉴定。通过搜索花生表达的序列标签(EST)和并行测序(454)库,我们确定了ahSad基因家族的三个成员。其中,只有一个基因ahSad3在种子发育过程中专门表达,并且完全对应于油脂积累。从异源四倍体花生中回收了两个ahSad3同源基因(ahSad3A和ahSad3B),并对其mRNA表达水平进行了表征。 ahSad3A和ahSad3B的开放阅读框是98%相同,由1158 bp组成,编码386个全氨基酸蛋白质,编码序列中有一个内含子。比较这两个同源基因的序列,发现在编码区有七个单核苷酸多态性和一个三联体插入。 Southern印迹分析表明,花生基因组中只有两个拷贝的ahSad3基因。同源基因特异性基因表达分析表明,两个ahSad3同源基因均在发育中的种子中表达,但基因表达明显偏向B基因组。我们的研究结果表明,ahSad3是可能的靶基因,可用于操纵低聚糖曲霉中的脂肪酸饱和度。

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